吡啶

The results showed that Kaidimycin was chemically neutral, macrocylic polylactones, stable and liable to dissolve into water and pyridine, slight to dissolve into methanol, ethanol and N-butanol, difficult to dissolve into ethyl acetate, acetone, benzene and chloroform. Chemical reaction of functional group of Kaidimycin showed that it had glycoside, amino acid and aldehyde, no reducing sugar, polypeptide and phenol.

凯地菌素属中等极性的、中性抗生素，极性纸层析结果与多烯类抗生素的纸层析结果相似：易溶于水、吡啶，微溶于甲醇、乙醇、正丁醇，不溶于乙酸乙酯、丙酮、苯、三氯化碳；对高温、光照和紫外处理有很好的稳定性；官能团反应试验结果发现，凯地菌素可能含有糖苷键、氨基酸伯氨基和醛基，不含有还原糖、多肽和酚基，高锰酸钾、浓硫酸反应与多烯大环内酯类抗生素的特性相似；并且依据纯品，采用生物法和分光光度法对摇床发酵液进行了效价的测定。

In the first chapter of the thesis we prepared the desired β-amino aicd ester at first,then throughstereoselective aldol condensation and lactamization we finished the synthesis of Plakoridine A lactam.

本论文中我们从β氨基酸衍生物出发，发展了一些构建多取代吡咯环和吡啶环的方法，并利用这些方法合成了一些具有重要生理活性的生物碱类天然产物。

Bromo-2-sulfolene (2) reacted with substituted benzoic acid salt s 3a～3c or alizarin yellow (3d) to give four novel allylic substitution products 4a～4d by esterification reaction, respectively.

以3，4-二溴环戊砜(1)为原料，在无水吡啶作用下发生消除反应，得到反应中间体4-溴-2-环戊烯砜(2)，再分别与一系列取代苯甲酸盐3a～3c以及茜素黄GG(3d)发生酯化反应，合成出4种新环戊烯砜衍生物4a～4d，并用IR，1HNMR，MS，元素分析等表征了它们的结构。

Cellulose benzoate,the degree of substitution of which was calculated from the content of C determined by element analysis,was prepared from microcrystalline celluloseand benzoyl chloride under heterogeneous condition and characterized by FT-IR and~1H-NMR.

研究了微晶纤维素和苯甲酰氯在多相条件下合成制备纤维素苯甲酸酯的反应，通过元素分析所得碳的质量百分含量计算了产物的取代度，并系统研究了吡啶与N，N-二甲基乙酰胺或与三乙胺混合反应溶剂、苯甲酰氯与纤维素羟基的摩尔比r、反应温度和反应时间对D S的影响，用FT-IR和1H-NM R对产物进行了表征。

There are three different nucleophilic reagent respectively reaction with m-dinitrobenzene ramification at distint alkaline term:With the nitrobenzene 、 m-nirtobenzenesulfone sodium salt 、 2.4-dinitro chlorobenzene 、 m-dinitrobenzene for bottom thing, benzyl cyanide、 benzyl chloride、 benzyl chloropyridine、is a nucleophilic reagent reaction for under the different term proceeds a series reaction. At the same time ,discuss about the impact factor to nucleophilicity such as the number of attract electron group、 ability of attract electron and the nucleophilic substitution reaction part.

设计了三类不同的亲核试剂分别与活化芳环在不同的碱性条件下发生反应：以苄基氰、苄基氯化吡啶为亲核试剂，以硝基苯、间二硝基苯、间硝基苯磺酸钠、2，4-二硝基苄基氯为底物进行亲核取代反应；并且对亲核试剂的体积效应、溶剂效应对亲核性影响，底物上吸电子基团的数目、吸电子能力对亲电性的影响，以及亲核取代反应的发生部位受哪些因素影响进行探讨。

The constant-volume combustion energy of 2-hydroxy-3,5-dinitropyridine lead salt(2HDNPPb) was determined by a precision rotating bomb calorimeter at 298.15K,which is equal to(-7 265.08±3.97)J/g.

利用精密转动弹热量计测定了2-羟基-3，5-二硝基吡啶铅盐(2HDNPPb)的燃烧能ΔcU，其结果为(-7 265.08±3.97)J/g。

Changing the acetate to other anions resulted in the loss of imprinting effect, suggesting that the complex formed prior to the polymerization was composed of copper, acetate, Alizarin and 2-vinylprindine.

研究还表明，在结合实验中，将醋酸根离子改变成其它阴离子，该聚合物就会失去分子识别能力，表明在聚合前的混合物中是由Cu，醋酸根离子，茜素和2-乙烯吡啶形成了配合物。

Methods:Using 10% OP and 10% TWEEN-20 as increasing dissoluble agents, andPAN as developing dye,the absorption of the complex compound of cadmium was measured at 555 nm. The content of the tracecadmium in water sample was determined.

分别以体积分数为10％OP和体积分数为10％吐温-20为增溶剂，以PAN1-(2-吡啶偶氮-2-萘酚为显色剂，在555nm波长处测定水中镉络合物的吸光度。

The fixation of CO2 carried out by these autotrophs, in addition to ATP, requires reduced pyridine nucleotide

除ATP外，由这些自养生物进行的CO2固定，需要还原的吡啶核苷酸。

In addition, there are a large number of strong hydrogenbondings(N-H…O,O-H…O) and weak hydrogen bondings in involving the cations,perchlorate counter-ions,PNOS and water molecules, which result in formation 3-D networkstructure.

晶体中Ni与配体希夫碱中的N 、N(吡吡啶醛类过渡金属希夫碱配合物的合成、晶体结构及谱学表征啶)、O原子配位形成变形的八面体构型，由于分子间，存在大量的强氢键和弱氢键，这些氢键的交互作用使得该配合物形成二维网状结构。

The split between the two groups can hardly be papered over.

这两个团体间的分歧难以掩饰。

This approach not only encourages a greater number of responses, but minimizes the likelihood of stale groupthink.

这种做法不仅鼓励了更多的反应，而且减少跟风的可能性。